| Weight | 64.057 g/mol |
|---|---|
| Formula | C4H9Li |
| Hydrogen Acceptors | 0 |
| Hydrogen Donors | 0 |
| Aromatic Rings | 0 |
| Rotatable Bonds | 1 |
N-butyllithium (109-72-8)
n-BuLi · tert-butyllithium
Score:
#304 in Materials science
,
#1951 in Physics
,
#6102 in Chemistry
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- Lithium intercalation via n-Butyllithium of the layered transition metal dichalcogenides (Materials Research Bulletin, 1975)
- Organometallic -complexes XII. The metalation of benzene and ferrocene by n-butyllithium-N,N,N,N-tetramethylethylenediamine (Journal of Organometallic Chemistry, 1967)
- Monomeric organolithium compounds in tetrahydrofuran: tert-butyllithium, sec-butyllithium, supermesityllithium, mesityllithium, and phenyllithium. Carbon-lithium coupling constants and the nature of carbon-lithium bonding (Organometallics, 1987)
- Brom/Lithium-Austausch an Vinylbromiden mit 2 Molquivv. tert-Butyllithium. Umsetzungen von Vinyllithiumverbindungen mit Hetero- und Kohlenstoff-Elektrophilen (Chemische Berichte, 1978)
- BromLithiumAustausch an Vinyl und Arylbromiden mit tertButyllithium Zur Ringerweiterung ber Dibromcarbenaddukte (Chemische Berichte, 1974)
- Clean and convenient procedure for converting primary alkyl iodides and .alpha.,.omega.-diiodoalkanes into the corresponding alkyllithium derivatives by treatment with tert-butyllithium (Journal of Organic Chemistry, 1990)
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Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - H225: Highly Flammable liquid and vapor
Danger Flammable liquids - Category 2 - H260: In contact with water releases flammable gases which may ignite spontaneously
Danger Substances And Mixtures Which, In Contact With Water, Emit Flammable Gases - Category 1 - n-BuLi
- tert-butyllithium
-
SMILES[Li+].CCC[CH2-]
-
InChIKeyDLEDOFVPSDKWEF-UHFFFAOYSA-N
- Pubchem - N-butyllithium
- Wikipedia - N-butyllithium
n-Butyllithium (abbreviated n-BuLi) is an organolithium reagent. It is widely used as a polymerization initiator in the production of elastomers such as polybutadiene or styrene-butadiene-styrene (SBS). Also, it is broadly employed as a strong base (superbase) in the synthesis of organic compounds as in the pharmaceutical industry.
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N-butyllithium
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